Variant report

Variant rs1239012
Chromosome Location chr2:168360705-168360706
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168338200-168366000 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:168341600-168365200 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr2:168355400-168361400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr2:168356600-168365200 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr2:168356800-168364400 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr2:168357000-168365400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr2:168358400-168365400 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:168359000-168361800 Weak transcription Fetal Lung lung
9 chr2:168360200-168361200 Enhancers HUVEC blood vessel
10 chr2:168360200-168361400 Enhancers Muscle Satellite Cultured Cells --
11 chr2:168360400-168361000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr2:168360400-168361600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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